AU666763B2 - Use of thiadiazole compounds as an antifouling active ingredient - Google Patents
Use of thiadiazole compounds as an antifouling active ingredient Download PDFInfo
- Publication number
- AU666763B2 AU666763B2 AU47400/93A AU4740093A AU666763B2 AU 666763 B2 AU666763 B2 AU 666763B2 AU 47400/93 A AU47400/93 A AU 47400/93A AU 4740093 A AU4740093 A AU 4740093A AU 666763 B2 AU666763 B2 AU 666763B2
- Authority
- AU
- Australia
- Prior art keywords
- biocide
- thiadiazole
- hydrogen
- weight
- halogen
- Prior art date
- Legal status (The legal status is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the status listed.)
- Ceased
Links
- 230000003373 anti-fouling effect Effects 0.000 title claims description 31
- 150000004867 thiadiazoles Chemical class 0.000 title claims description 8
- 239000004480 active ingredient Substances 0.000 title description 6
- 239000003973 paint Substances 0.000 claims description 31
- 239000000203 mixture Substances 0.000 claims description 30
- 239000003139 biocide Substances 0.000 claims description 29
- 230000003115 biocidal effect Effects 0.000 claims description 27
- 239000001257 hydrogen Substances 0.000 claims description 27
- 229910052739 hydrogen Inorganic materials 0.000 claims description 27
- -1 carboxy, hydroxy Chemical group 0.000 claims description 21
- 229910052736 halogen Inorganic materials 0.000 claims description 21
- 238000000034 method Methods 0.000 claims description 20
- 150000001875 compounds Chemical class 0.000 claims description 19
- 125000004432 carbon atom Chemical group C* 0.000 claims description 18
- 150000002367 halogens Chemical class 0.000 claims description 17
- 125000000217 alkyl group Chemical group 0.000 claims description 14
- 238000009472 formulation Methods 0.000 claims description 13
- 125000000547 substituted alkyl group Chemical group 0.000 claims description 13
- 150000002431 hydrogen Chemical class 0.000 claims description 12
- 239000000049 pigment Substances 0.000 claims description 12
- UFHFLCQGNIYNRP-UHFFFAOYSA-N Hydrogen Chemical compound [H][H] UFHFLCQGNIYNRP-UHFFFAOYSA-N 0.000 claims description 10
- 239000011230 binding agent Substances 0.000 claims description 10
- 125000005843 halogen group Chemical group 0.000 claims description 9
- 125000000449 nitro group Chemical group [O-][N+](*)=O 0.000 claims description 8
- 125000003545 alkoxy group Chemical group 0.000 claims description 6
- 125000004093 cyano group Chemical group *C#N 0.000 claims description 6
- FJWGRXKOBIVTFA-UHFFFAOYSA-N 2,3-dibromobutanedioic acid Chemical compound OC(=O)C(Br)C(Br)C(O)=O FJWGRXKOBIVTFA-UHFFFAOYSA-N 0.000 claims description 4
- 125000004435 hydrogen atom Chemical group [H]* 0.000 claims description 4
- JLHMJWHSBYZWJJ-UHFFFAOYSA-N 1,2-thiazole 1-oxide Chemical compound O=S1C=CC=N1 JLHMJWHSBYZWJJ-UHFFFAOYSA-N 0.000 claims description 3
- 229940099451 3-iodo-2-propynylbutylcarbamate Drugs 0.000 claims description 3
- WYVVKGNFXHOCQV-UHFFFAOYSA-N 3-iodoprop-2-yn-1-yl butylcarbamate Chemical compound CCCCNC(=O)OCC#CI WYVVKGNFXHOCQV-UHFFFAOYSA-N 0.000 claims description 3
- LKGIJQSLJASXHQ-UHFFFAOYSA-N 5-methylsulfonyl-3-phenyl-1,2,4-thiadiazole Chemical group S1C(S(=O)(=O)C)=NC(C=2C=CC=CC=2)=N1 LKGIJQSLJASXHQ-UHFFFAOYSA-N 0.000 claims description 3
- YKSNLCVSTHTHJA-UHFFFAOYSA-L maneb Chemical compound [Mn+2].[S-]C(=S)NCCNC([S-])=S YKSNLCVSTHTHJA-UHFFFAOYSA-L 0.000 claims description 3
- 230000005789 organism growth Effects 0.000 claims description 3
- VLLMWSRANPNYQX-UHFFFAOYSA-N thiadiazole Chemical compound C1=CSN=N1.C1=CSN=N1 VLLMWSRANPNYQX-UHFFFAOYSA-N 0.000 claims description 3
- 229940043810 zinc pyrithione Drugs 0.000 claims description 3
- PICXIOQBANWBIZ-UHFFFAOYSA-N zinc;1-oxidopyridine-2-thione Chemical compound [Zn+2].[O-]N1C=CC=CC1=S.[O-]N1C=CC=CC1=S PICXIOQBANWBIZ-UHFFFAOYSA-N 0.000 claims description 3
- LVUOLMAWRDSAHJ-UHFFFAOYSA-N 5-methylsulfonyl-3-(4-nitrophenyl)-1,2,4-thiadiazole Chemical compound S1C(S(=O)(=O)C)=NC(C=2C=CC(=CC=2)[N+]([O-])=O)=N1 LVUOLMAWRDSAHJ-UHFFFAOYSA-N 0.000 claims description 2
- 125000003178 carboxy group Chemical group [H]OC(*)=O 0.000 claims description 2
- CRQQGFGUEAVUIL-UHFFFAOYSA-N chlorothalonil Chemical group ClC1=C(Cl)C(C#N)=C(Cl)C(C#N)=C1Cl CRQQGFGUEAVUIL-UHFFFAOYSA-N 0.000 claims description 2
- 125000002887 hydroxy group Chemical group [H]O* 0.000 claims description 2
- HCHKCACWOHOZIP-UHFFFAOYSA-N Zinc Chemical compound [Zn] HCHKCACWOHOZIP-UHFFFAOYSA-N 0.000 claims 4
- 239000011701 zinc Substances 0.000 claims 4
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- DYALFOTWKUYHSX-UHFFFAOYSA-N 3-(4-methylphenyl)-5-methylsulfonyl-1,2,4-thiadiazole Chemical compound C1=CC(C)=CC=C1C1=NSC(S(C)(=O)=O)=N1 DYALFOTWKUYHSX-UHFFFAOYSA-N 0.000 claims 2
- 238000000576 coating method Methods 0.000 claims 2
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- 239000013535 sea water Substances 0.000 claims 2
- ORBXTMQSELDISK-UHFFFAOYSA-N 2-n-tert-butyl-1-n-cyclopropyl-4-methylsulfanyl-2h-1,3,5-triazine-1,2-diamine Chemical compound C1=NC(SC)=NC(NC(C)(C)C)N1NC1CC1 ORBXTMQSELDISK-UHFFFAOYSA-N 0.000 claims 1
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- 239000000969 carrier Substances 0.000 description 1
- 239000012876 carrier material Substances 0.000 description 1
- 239000005018 casein Substances 0.000 description 1
- BECPQYXYKAMYBN-UHFFFAOYSA-N casein, tech. Chemical compound NCCCCC(C(O)=O)N=C(O)C(CC(O)=O)N=C(O)C(CCC(O)=N)N=C(O)C(CC(C)C)N=C(O)C(CCC(O)=O)N=C(O)C(CC(O)=O)N=C(O)C(CCC(O)=O)N=C(O)C(C(C)O)N=C(O)C(CCC(O)=N)N=C(O)C(CCC(O)=N)N=C(O)C(CCC(O)=N)N=C(O)C(CCC(O)=O)N=C(O)C(CCC(O)=O)N=C(O)C(COP(O)(O)=O)N=C(O)C(CCC(O)=N)N=C(O)C(N)CC1=CC=CC=C1 BECPQYXYKAMYBN-UHFFFAOYSA-N 0.000 description 1
- 235000021240 caseins Nutrition 0.000 description 1
- 150000008280 chlorinated hydrocarbons Chemical class 0.000 description 1
- 229910052801 chlorine Inorganic materials 0.000 description 1
- 238000010276 construction Methods 0.000 description 1
- 238000007334 copolymerization reaction Methods 0.000 description 1
- 150000001879 copper Chemical class 0.000 description 1
- 229910052802 copper Inorganic materials 0.000 description 1
- 239000010949 copper Substances 0.000 description 1
- 150000001880 copper compounds Chemical class 0.000 description 1
- DOBRDRYODQBAMW-UHFFFAOYSA-N copper(i) cyanide Chemical compound [Cu+].N#[C-] DOBRDRYODQBAMW-UHFFFAOYSA-N 0.000 description 1
- BQVVSSAWECGTRN-UHFFFAOYSA-L copper;dithiocyanate Chemical compound [Cu+2].[S-]C#N.[S-]C#N BQVVSSAWECGTRN-UHFFFAOYSA-L 0.000 description 1
- GUJOJGAPFQRJSV-UHFFFAOYSA-N dialuminum;dioxosilane;oxygen(2-);hydrate Chemical compound O.[O-2].[O-2].[O-2].[Al+3].[Al+3].O=[Si]=O.O=[Si]=O.O=[Si]=O.O=[Si]=O GUJOJGAPFQRJSV-UHFFFAOYSA-N 0.000 description 1
- 150000001989 diazonium salts Chemical class 0.000 description 1
- 125000004177 diethyl group Chemical group [H]C([H])([H])C([H])([H])* 0.000 description 1
- USIUVYZYUHIAEV-UHFFFAOYSA-N diphenyl ether Chemical class C=1C=CC=CC=1OC1=CC=CC=C1 USIUVYZYUHIAEV-UHFFFAOYSA-N 0.000 description 1
- 239000006185 dispersion Substances 0.000 description 1
- 238000004090 dissolution Methods 0.000 description 1
- 238000005553 drilling Methods 0.000 description 1
- 239000000975 dye Substances 0.000 description 1
- 239000003995 emulsifying agent Substances 0.000 description 1
- 239000000839 emulsion Substances 0.000 description 1
- 150000002118 epoxides Chemical class 0.000 description 1
- 230000032050 esterification Effects 0.000 description 1
- 238000005886 esterification reaction Methods 0.000 description 1
- 239000000706 filtrate Substances 0.000 description 1
- 125000001153 fluoro group Chemical group F* 0.000 description 1
- 230000022244 formylation Effects 0.000 description 1
- 238000006170 formylation reaction Methods 0.000 description 1
- 239000000446 fuel Substances 0.000 description 1
- 150000004820 halides Chemical class 0.000 description 1
- 230000026030 halogenation Effects 0.000 description 1
- 238000005658 halogenation reaction Methods 0.000 description 1
- FUZZWVXGSFPDMH-UHFFFAOYSA-N hexanoic acid Chemical compound CCCCCC(O)=O FUZZWVXGSFPDMH-UHFFFAOYSA-N 0.000 description 1
- 229930195733 hydrocarbon Natural products 0.000 description 1
- 150000002430 hydrocarbons Chemical class 0.000 description 1
- ZMZDMBWJUHKJPS-UHFFFAOYSA-N hydrogen thiocyanate Natural products SC#N ZMZDMBWJUHKJPS-UHFFFAOYSA-N 0.000 description 1
- 230000003301 hydrolyzing effect Effects 0.000 description 1
- CJXJAUKCHHAJQN-UHFFFAOYSA-N hydron;4-nitrobenzenecarboximidamide;chloride Chemical compound Cl.NC(=N)C1=CC=C([N+]([O-])=O)C=C1 CJXJAUKCHHAJQN-UHFFFAOYSA-N 0.000 description 1
- 239000012442 inert solvent Substances 0.000 description 1
- 125000002346 iodo group Chemical group I* 0.000 description 1
- 239000004571 lime Substances 0.000 description 1
- 238000012423 maintenance Methods 0.000 description 1
- 125000005641 methacryl group Chemical group 0.000 description 1
- 229920003145 methacrylic acid copolymer Polymers 0.000 description 1
- 150000004704 methoxides Chemical class 0.000 description 1
- WCYWZMWISLQXQU-UHFFFAOYSA-N methyl Chemical class [CH3] WCYWZMWISLQXQU-UHFFFAOYSA-N 0.000 description 1
- 125000002496 methyl group Chemical group [H]C([H])([H])* 0.000 description 1
- 125000000325 methylidene group Chemical group [H]C([H])=* 0.000 description 1
- 229910052901 montmorillonite Inorganic materials 0.000 description 1
- GEMHFKXPOCTAIP-UHFFFAOYSA-N n,n-dimethyl-n'-phenylcarbamimidoyl chloride Chemical compound CN(C)C(Cl)=NC1=CC=CC=C1 GEMHFKXPOCTAIP-UHFFFAOYSA-N 0.000 description 1
- 150000002790 naphthalenes Chemical class 0.000 description 1
- 230000000802 nitrating effect Effects 0.000 description 1
- 238000006396 nitration reaction Methods 0.000 description 1
- 150000002825 nitriles Chemical class 0.000 description 1
- 229910052757 nitrogen Inorganic materials 0.000 description 1
- 238000010534 nucleophilic substitution reaction Methods 0.000 description 1
- 239000003960 organic solvent Substances 0.000 description 1
- 150000003961 organosilicon compounds Chemical class 0.000 description 1
- 239000007800 oxidant agent Substances 0.000 description 1
- 230000003647 oxidation Effects 0.000 description 1
- 238000007254 oxidation reaction Methods 0.000 description 1
- 229910052763 palladium Inorganic materials 0.000 description 1
- 239000012188 paraffin wax Substances 0.000 description 1
- 230000000361 pesticidal effect Effects 0.000 description 1
- 239000003209 petroleum derivative Substances 0.000 description 1
- 125000001997 phenyl group Chemical group [H]C1=C([H])C([H])=C(*)C([H])=C1[H] 0.000 description 1
- XNGIFLGASWRNHJ-UHFFFAOYSA-L phthalate(2-) Chemical compound [O-]C(=O)C1=CC=CC=C1C([O-])=O XNGIFLGASWRNHJ-UHFFFAOYSA-L 0.000 description 1
- 229920003023 plastic Polymers 0.000 description 1
- 239000004033 plastic Substances 0.000 description 1
- 239000004014 plasticizer Substances 0.000 description 1
- 229910052697 platinum Inorganic materials 0.000 description 1
- 229920002432 poly(vinyl methyl ether) polymer Polymers 0.000 description 1
- 239000004584 polyacrylic acid Substances 0.000 description 1
- 229920000728 polyester Polymers 0.000 description 1
- 229920000193 polymethacrylate Polymers 0.000 description 1
- 239000001205 polyphosphate Substances 0.000 description 1
- 235000011176 polyphosphates Nutrition 0.000 description 1
- 229920002635 polyurethane Polymers 0.000 description 1
- 239000004814 polyurethane Substances 0.000 description 1
- 229920002451 polyvinyl alcohol Polymers 0.000 description 1
- 235000019422 polyvinyl alcohol Nutrition 0.000 description 1
- 229920001289 polyvinyl ether Polymers 0.000 description 1
- 239000011591 potassium Substances 0.000 description 1
- 229910052700 potassium Inorganic materials 0.000 description 1
- TYJJADVDDVDEDZ-UHFFFAOYSA-M potassium hydrogencarbonate Chemical compound [K+].OC([O-])=O TYJJADVDDVDEDZ-UHFFFAOYSA-M 0.000 description 1
- BDAWXSQJJCIFIK-UHFFFAOYSA-N potassium methoxide Chemical compound [K+].[O-]C BDAWXSQJJCIFIK-UHFFFAOYSA-N 0.000 description 1
- 230000001681 protective effect Effects 0.000 description 1
- 238000000746 purification Methods 0.000 description 1
- 238000001953 recrystallisation Methods 0.000 description 1
- 150000003839 salts Chemical class 0.000 description 1
- 150000004756 silanes Chemical class 0.000 description 1
- 150000004760 silicates Chemical class 0.000 description 1
- 239000011734 sodium Substances 0.000 description 1
- 229910052708 sodium Inorganic materials 0.000 description 1
- SUBJHSREKVAVAR-UHFFFAOYSA-N sodium;methanol;methanolate Chemical compound [Na+].OC.[O-]C SUBJHSREKVAVAR-UHFFFAOYSA-N 0.000 description 1
- 239000000243 solution Substances 0.000 description 1
- 239000007858 starting material Substances 0.000 description 1
- 125000001424 substituent group Chemical group 0.000 description 1
- 229940124530 sulfonamide Drugs 0.000 description 1
- 150000003456 sulfonamides Chemical class 0.000 description 1
- 239000010936 titanium Substances 0.000 description 1
- 229910052719 titanium Inorganic materials 0.000 description 1
- LPUCKLOWOWADAC-UHFFFAOYSA-M tributylstannyl 2-methylprop-2-enoate Chemical compound CCCC[Sn](CCCC)(CCCC)OC(=O)C(C)=C LPUCKLOWOWADAC-UHFFFAOYSA-M 0.000 description 1
- 229960001124 trientine Drugs 0.000 description 1
- 235000013311 vegetables Nutrition 0.000 description 1
Classifications
-
- C—CHEMISTRY; METALLURGY
- C09—DYES; PAINTS; POLISHES; NATURAL RESINS; ADHESIVES; COMPOSITIONS NOT OTHERWISE PROVIDED FOR; APPLICATIONS OF MATERIALS NOT OTHERWISE PROVIDED FOR
- C09D—COATING COMPOSITIONS, e.g. PAINTS, VARNISHES OR LACQUERS; FILLING PASTES; CHEMICAL PAINT OR INK REMOVERS; INKS; CORRECTING FLUIDS; WOODSTAINS; PASTES OR SOLIDS FOR COLOURING OR PRINTING; USE OF MATERIALS THEREFOR
- C09D5/00—Coating compositions, e.g. paints, varnishes or lacquers, characterised by their physical nature or the effects produced; Filling pastes
- C09D5/16—Antifouling paints; Underwater paints
- C09D5/1606—Antifouling paints; Underwater paints characterised by the anti-fouling agent
- C09D5/1612—Non-macromolecular compounds
- C09D5/1625—Non-macromolecular compounds organic
-
- A—HUMAN NECESSITIES
- A01—AGRICULTURE; FORESTRY; ANIMAL HUSBANDRY; HUNTING; TRAPPING; FISHING
- A01N—PRESERVATION OF BODIES OF HUMANS OR ANIMALS OR PLANTS OR PARTS THEREOF; BIOCIDES, e.g. AS DISINFECTANTS, AS PESTICIDES OR AS HERBICIDES; PEST REPELLANTS OR ATTRACTANTS; PLANT GROWTH REGULATORS
- A01N43/00—Biocides, pest repellants or attractants, or plant growth regulators containing heterocyclic compounds
- A01N43/72—Biocides, pest repellants or attractants, or plant growth regulators containing heterocyclic compounds having rings with nitrogen atoms and oxygen or sulfur atoms as ring hetero atoms
- A01N43/82—Biocides, pest repellants or attractants, or plant growth regulators containing heterocyclic compounds having rings with nitrogen atoms and oxygen or sulfur atoms as ring hetero atoms five-membered rings with three ring hetero atoms
Landscapes
- Life Sciences & Earth Sciences (AREA)
- Wood Science & Technology (AREA)
- Chemical & Material Sciences (AREA)
- Engineering & Computer Science (AREA)
- Plant Pathology (AREA)
- General Health & Medical Sciences (AREA)
- Agronomy & Crop Science (AREA)
- Pest Control & Pesticides (AREA)
- Materials Engineering (AREA)
- Health & Medical Sciences (AREA)
- Dentistry (AREA)
- Organic Chemistry (AREA)
- Zoology (AREA)
- Environmental Sciences (AREA)
- Agricultural Chemicals And Associated Chemicals (AREA)
- Paints Or Removers (AREA)
- Lubricants (AREA)
- Plural Heterocyclic Compounds (AREA)
- Nitrogen- Or Sulfur-Containing Heterocyclic Ring Compounds With Rings Of Six Or More Members (AREA)
Applications Claiming Priority (2)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| DE4230955 | 1992-09-16 | ||
| DE4230955A DE4230955A1 (de) | 1992-09-16 | 1992-09-16 | Verwendung von Thiadiazol-Verbindungen als Antifouling-Wirkstoff |
Publications (2)
| Publication Number | Publication Date |
|---|---|
| AU4740093A AU4740093A (en) | 1994-03-24 |
| AU666763B2 true AU666763B2 (en) | 1996-02-22 |
Family
ID=6468078
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| AU47400/93A Ceased AU666763B2 (en) | 1992-09-16 | 1993-09-16 | Use of thiadiazole compounds as an antifouling active ingredient |
Country Status (12)
| Country | Link |
|---|---|
| US (1) | US5332430A (tr) |
| EP (1) | EP0588007B1 (tr) |
| JP (1) | JPH06211609A (tr) |
| AU (1) | AU666763B2 (tr) |
| CA (1) | CA2106287C (tr) |
| DE (2) | DE4230955A1 (tr) |
| DK (1) | DK0588007T3 (tr) |
| ES (1) | ES2093328T3 (tr) |
| FI (1) | FI934064A (tr) |
| GR (1) | GR3021267T3 (tr) |
| MX (1) | MX9305705A (tr) |
| NO (1) | NO303861B1 (tr) |
Families Citing this family (10)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US5472993A (en) * | 1994-12-30 | 1995-12-05 | Korea Chemical Co., Ltd. | Anti-fouling paint |
| NO952270D0 (no) * | 1995-06-08 | 1995-06-08 | Jotun As | Polymerer for grohemmende maling og fremgangsmåte for fremstilling derav |
| EP0841353A1 (de) | 1996-11-07 | 1998-05-13 | Witco GmbH | Verfahren zur Herstellung von polymeren Bindemitteln und deren Verwendung für Antifouling-Anstrichsysteme |
| DK0841380T3 (da) * | 1996-11-07 | 2000-02-21 | Witco Gmbh | Fremgangsmåde til fremstilling af polymere bindemidler samt disses anvendelse i antifouling-farvesystemer |
| DE10209934A1 (de) * | 2002-03-07 | 2003-10-02 | Beta Tec Hopfenprodukte Gmbh | Verfahren zur Kontrolle von biologischen Prozessen in Wasser |
| US20040101539A1 (en) * | 2002-11-22 | 2004-05-27 | Ernst Engler | Aqueous dispersion of low-melting organic solids |
| DE102005011990A1 (de) * | 2005-03-14 | 2006-09-21 | Basf Ag | Foulingresistente Polyurethane, insbesondere für maritime Anwendungen |
| JP5360759B2 (ja) * | 2009-06-08 | 2013-12-04 | 日東化成株式会社 | 防汚塗料組成物、該組成物を用いて形成される防汚塗膜、該塗膜を表面に有する塗装物、および該塗膜を形成する防汚処理方法 |
| SG11201601497PA (en) * | 2013-08-31 | 2016-04-28 | Houghton Technical Corp | Hydraulic fluid compositions |
| EP3283542A4 (en) | 2015-04-15 | 2018-08-22 | Houghton Technical Corp. | Compositions and methods of using polyamidopolyamines and non-polymeric amidoamines |
Citations (3)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| GB1356391A (en) * | 1970-09-09 | 1974-06-12 | Fisons Ltd | Pesticides |
| US3917630A (en) * | 1971-08-31 | 1975-11-04 | Ciba Geigy Corp | Heterocyclic compounds |
| EP0534219A1 (de) * | 1991-09-19 | 1993-03-31 | Bayer Ag | 3-(4-Bromphenyl)-5-methylsulfonyl-1,2,4-thiadiazol, ein Verfahren zur Herstellung, seine Verwendung und neue Zwischenprodukte |
Family Cites Families (9)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| CA588046A (en) * | 1959-12-01 | S. Karsten Kenneth | Wax compositions containing a mercaptobenzothiazole as a microbicide | |
| US3597426A (en) * | 1968-10-02 | 1971-08-03 | M & T Chemicals Inc | Unsymmetrical disubstituted perthiocyanates |
| DE2242187A1 (de) * | 1971-08-31 | 1973-03-08 | Ciba Geigy Ag | Heterocyclische verbindungen |
| AR207229A1 (es) * | 1973-08-20 | 1976-09-22 | Rohm & Haas | Composicion de recubrimiento estabilizada con formaldehido y metodo para su preparacion |
| JPS519705A (ja) * | 1974-07-15 | 1976-01-26 | Taiyo Kagaku Kogyo Co Ltd | Mokuzainobokabiho |
| US4209522A (en) * | 1978-06-28 | 1980-06-24 | The Dow Chemical Company | Antimicrobial bis(5-nitro-2-thiazolyl)thioisothiazoles and thiadiazoles |
| US4711915A (en) * | 1986-04-07 | 1987-12-08 | R. T. Vanderbilt Company, Inc. | Surface coating compositions containing substituted 1,3,4-thiadiazoles |
| DE3722320A1 (de) * | 1987-07-07 | 1989-01-19 | Bayer Ag | Mikrobizide mittel |
| JPH02173165A (ja) * | 1988-12-27 | 1990-07-04 | Nippon Soda Co Ltd | 防汚剤 |
-
1992
- 1992-09-16 DE DE4230955A patent/DE4230955A1/de not_active Withdrawn
-
1993
- 1993-07-10 EP EP93111095A patent/EP0588007B1/de not_active Expired - Lifetime
- 1993-07-10 ES ES93111095T patent/ES2093328T3/es not_active Expired - Lifetime
- 1993-07-10 DK DK93111095.1T patent/DK0588007T3/da active
- 1993-07-10 DE DE59303733T patent/DE59303733D1/de not_active Expired - Lifetime
- 1993-09-14 JP JP5228678A patent/JPH06211609A/ja active Pending
- 1993-09-15 CA CA002106287A patent/CA2106287C/en not_active Expired - Fee Related
- 1993-09-15 NO NO933286A patent/NO303861B1/no unknown
- 1993-09-15 US US08/123,185 patent/US5332430A/en not_active Expired - Fee Related
- 1993-09-16 FI FI934064A patent/FI934064A/fi unknown
- 1993-09-16 AU AU47400/93A patent/AU666763B2/en not_active Ceased
- 1993-09-17 MX MX9305705A patent/MX9305705A/es not_active IP Right Cessation
-
1996
- 1996-10-04 GR GR960402619T patent/GR3021267T3/el unknown
Patent Citations (3)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| GB1356391A (en) * | 1970-09-09 | 1974-06-12 | Fisons Ltd | Pesticides |
| US3917630A (en) * | 1971-08-31 | 1975-11-04 | Ciba Geigy Corp | Heterocyclic compounds |
| EP0534219A1 (de) * | 1991-09-19 | 1993-03-31 | Bayer Ag | 3-(4-Bromphenyl)-5-methylsulfonyl-1,2,4-thiadiazol, ein Verfahren zur Herstellung, seine Verwendung und neue Zwischenprodukte |
Also Published As
| Publication number | Publication date |
|---|---|
| NO303861B1 (no) | 1998-09-14 |
| ES2093328T3 (es) | 1996-12-16 |
| FI934064A0 (fi) | 1993-09-16 |
| CA2106287A1 (en) | 1994-03-17 |
| GR3021267T3 (en) | 1997-01-31 |
| FI934064A (fi) | 1994-03-17 |
| AU4740093A (en) | 1994-03-24 |
| DK0588007T3 (tr) | 1997-02-24 |
| DE4230955A1 (de) | 1994-03-17 |
| CA2106287C (en) | 1997-07-01 |
| JPH06211609A (ja) | 1994-08-02 |
| NO933286L (no) | 1994-03-17 |
| MX9305705A (es) | 1994-05-31 |
| EP0588007A1 (de) | 1994-03-23 |
| NO933286D0 (no) | 1993-09-15 |
| EP0588007B1 (de) | 1996-09-11 |
| US5332430A (en) | 1994-07-26 |
| DE59303733D1 (de) | 1996-10-17 |
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Legal Events
| Date | Code | Title | Description |
|---|---|---|---|
| MK14 | Patent ceased section 143(a) (annual fees not paid) or expired |